Canonical Allele Identifier: CA2210140399

Gene: ABCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16154620G= , CM000678.2:g.16154620G=	GRCh38
NC_000016.9:g.16248477G= , CM000678.1:g.16248477G=	GRCh37
NC_000016.8:g.16155978G=	NCBI36
NG_007558.2:g.73852C=
NG_007558.3:g.73998C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.*380+8C=	ENSP00000483331.2:n.*380+8C=
ENST00000205557.12:c.4208+8C= MANE Select	ENSP00000205557.7:n.4208+8C=
ENST00000640696.1:c.1022+8C=	ENSP00000492197.1:n.1022+8C=
ENST00000205557.11:c.4208+8C=	ENSP00000205557.7:n.4208+8C=
ENST00000456970.6:c.3833+8C=	ENSP00000405002.2:n.3833+8C=
ENST00000576204.5:n.1071+8C=
ENST00000622290.4:c.*1417+8C=	ENSP00000483331.1:n.*1417+8C=
NM_001171.5:c.4208+8C=	NP_001162.4:n.4208+8C=
XM_011522479.1:c.4175+8C=	XP_011520781.1:n.4175+8C=
XM_011522480.1:c.3866+8C=	XP_011520782.1:n.3866+8C=
XM_011522481.1:c.3866+8C=	XP_011520783.1:n.3866+8C=
XR_933134.1:n.539-5161G=
NM_001351800.1:c.3866+8C=	NP_001338729.1:n.3866+8C=
NR_147784.1:n.3870+8C=
XM_011522479.2:c.4175+8C=	XP_011520781.1:n.4175+8C=
XM_011522481.3:c.3866+8C=	XP_011520783.1:n.3866+8C=
XM_017023212.1:c.4040+8C=	XP_016878701.1:n.4040+8C=
XM_024450261.1:c.4244+8C=	XP_024306029.1:n.4244+8C=
NM_001171.6:c.4208+8C= MANE Select	NP_001162.5:n.4208+8C=